Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.
- DOI
- 10.1186/s13023-026-04497-x
- Published
- 2026 Jul 21
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- unknown
Credibility signals
limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04497-x,
title = {Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.},
author = {Coursimault J and Guillon E and Lecoquierre F and Charbonnier C and Guerrot AM and Goldenberg A and Nicolas G and Schaefer E and Ayrolles A and Delorme R and Riccardi F and Grelet M and Caumes R and Nizon M and Isidor B and Jouret G and Rooryck C and Amiel J and Alaix AS and Morel V and Jacquinet A and Mignot C and Faivre L and Fraile-Caietta E and Chalopin S and Dubern B and Poitou C},
year = {2026},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-026-04497-x},
url = {https://doi.org/10.1186/s13023-026-04497-x}
}RIS
TY - JOUR TI - Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires. AU - Coursimault J AU - Guillon E AU - Lecoquierre F AU - Charbonnier C AU - Guerrot AM AU - Goldenberg A AU - Nicolas G AU - Schaefer E AU - Ayrolles A AU - Delorme R AU - Riccardi F AU - Grelet M AU - Caumes R AU - Nizon M AU - Isidor B AU - Jouret G AU - Rooryck C AU - Amiel J AU - Alaix AS AU - Morel V AU - Jacquinet A AU - Mignot C AU - Faivre L AU - Fraile-Caietta E AU - Chalopin S AU - Dubern B AU - Poitou C PY - 2026 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-026-04497-x UR - https://doi.org/10.1186/s13023-026-04497-x ER -
APA
J, C., E, G., F, L., C, C., AM, G., A, G., G, N., E, S., A, A., R, D., F, R., M, G., R, C., M, N., B, I., G, J., C, R., J, A., AS, A., V, M., A, J., C, M., L, F., E, F., S, C., B, D., & C, P. (2026). Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04497-x
Source records
- pubmed · retrieved 2026-09-26T14:55:24.549Z